10. Which of the following solvent is the most soluble in water?
(A) hexanoic acid
(B) dichloromethane
(C) dimethylformamide
(D) 1-butanol
(E) ethyl acetate

6. Consider a system in which an ester is hydrolyzed in a base catalyzed hydrolysis using potassium hydroxide as the base. After the reaction, what will happen theoretically concerning the acidity of the reaction mixture when compared to the beginning of the reaction? (A) The mixture will become more basic compared to the beginning. (B) The mixture will become more acidic compared to the beginning. (C) The acidity of the reaction mixture will not change. (D) The concept of acidity cannot be applied to organic system. (E) The exact situations depend on the actual structure of the ester.

7. Which of the following position is the most reactive towards electrophilic aromatic substitution? (A)A(B)B(C)C(D)D(E)E

8. Describe the number of signals and their splitting in the 1H NMR of the following compound: (A) 7 signals: 1 singlet, 2 doublets, 1 triplet, 3 quartet (B) 6 signals: 1 singlet, 3 doublets, 1 triplet, 1 quartet (C) 7 signals: 4 doublets, 2 triplet, 1 quartet (D) 7 signals: 1 singlet, 4 doublets, 1 triplet, 1 quartet (E) 8 signals: 2 singlet, 4 doublets, 1 triplet, 1 quartet

9.Which of the following pair of structures represent an identical compound? (A)(B)(C)(D)(E)

11. Which of the following compound is the most reactive in an SN1 reaction? (A)(B)(C)(D)(E)

12. Which of the following reaction conditions will give the desire product as shown? Reaction conditions: (1)O3 (2) (3) Excess HBr, then excess KOH (4) BuLi, then H2O (A) (1) and (2) only (B) (2) and (3) only (C) (2), (3) and (4) only (D) All of the above (E) None of the above

13. Which of the following amine CANNOT be synthesized by reductive amination? (A)(B)(C)(D)(E)

14. Which of the following acetal will react the fastest in acid-catalyzed hydrolysis? (A)(B)(C)(D)(E)

15. Which of the following compounds is the oxidant in the reaction below? (A)(B)(C)KOH(D)oxygen in air(E)

16. Rank the reactivity of the following compounds towards nucleophilic substitution of carboxylic acid derivative in increasing order (least to most). (A)2＜3＜5＜1＜4 (B)5＜3＜2＜4＜1 (C)1＜2＜5＜3＜4 (D)1＜2＜3＜5＜4 (E)2＜5＜3＜1＜4